Journals / Turkish Journal of Hematology / 2020 / Cilt: 37 - Sayı: 2

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia

Bir Beta Talasemi İntermedya Hastasında İki Nadir Patojenik HBB Varyantı

Pages
135–136
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
🔖

Cite This Article

BÜYÜKDOĞAN, M., HANÇER, V. S., FIŞGIN, T. (2022). Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia. Turkish Journal of Hematology, Cilt: 37 - Sayı: 2, 135–136. https://ajindex.com/articles/606623

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Rachmilewitz EA, Giardina PJ. How I treat thalassemia. Blood 2011;118:3479- 3488
  2. Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 3rd ed. Oxford, Blackwell Scientific Publications, 1981
  3. World Health Organization. Management of Haemoglobin Disorders: Report of Joint WHO-TIF Meeting. Geneva, WHO, 2012
  4. Atanasovska B, Bozhinovski G, Chakalova L, Kocheva S, Karanfilski O, Plaseska-Karanfiska D. Molecular diagnostics of β-thalassemia. Balkan J Med Genet 2012;15:61-65
  5. Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis 2010; 5:11
  6. NCBI. dbSNP. Available at www.ncbi.nlm.nih.gov/snp
  7. Altay C, Basak AN. Molecular basis and prenatal diagnosis of hemoglobinopathies in Turkey. Int J Peadiatr Hematol Oncol 1995;2:283- 290
  8. Al-Allawi NA, Al-Mousawi BM, Badi AI, Jalal SD. The spectrum of β-thalassemia mutations in Baghdad, Central Iraq. Hemoglobin 2013;37:444-453
  9. Çürük MA, Arpacı A, Atilla G, Tuli A, Kılınç Y, Aksoy K, Yüreğir GT. Genetic heterogeneity of β thalassemia at Çukurova in Southern Turkey. Hemoglobin 2001;25:241-245
  10. Al-Allawi NA, Jalal SD, Mohammad AD, Omer SQ, Markous RS. β-Thalassemia intermedia in northern Iraq: a single center experience. Biomed Res Int 2014;2014:262853.